Role DescriptionRecently we set up a new QA operations team to focus on finding a cure. By putting together a team of different professionals with different skills we are bundling our strength to. As a QA specialist you will be our newest addition to this newly created team. Because of the diversity it is very important to work cross functionally. You will assist with different kind of tasks according to the GMP regulations.
ResponsibilitiesAs a part of the QA operations team you will be responsible for: - Continually improving the project according to the lean method - The quality and performance of the deviations, CAPAs, batch reviews and complaint management - Ensuring a fluent process and the result of the packaging, shipping and disposition process - Assisting with the implementation and maintenance of the GMP training system - Contact management with cooperating companies though Europe
RequirementsYou have: - A BSc in biological sciences - Experience within the pharmaceutical or biotechnological industry (at least 3 years) - Experience with change control (at least 1 year) - Knowledge of current GMP regulations - Experience with the Lean way of working - Experience in performing batch reviews, CAPA's and deviations - A team spirit and a creative way of thinking
Other informationYou will be working in a welcoming team and a welcoming company. In addition to financially we will invest in you in a personal way by giving you the possibility to develop yourself and express your ideas.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.